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G11.3 - Cerebellar ataxia with defective DNA repair


The ICD 10 Code for Cerebellar ataxia with defective DNA repair is listed as G11.3.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field Value
Diagnosis Code: G11.3
Description: Cerebellar ataxia with defective DNA repair
  • Ataxia telangiectasia [Louis-Bar]
  • Excludes2: Cockayne's syndrome (Q87.1)
  • other disorders of purine and pyrimidine metabolism (E79.-)
  • xeroderma pigmentosum (Q82.1)
Diagnostic Related Groups
(MS-DRG v30.0)
058 - Multiple Sclerosis & Cerebellar Ataxia W Mcc
059 - Multiple Sclerosis & Cerebellar Ataxia W Cc
060 - Multiple Sclerosis & Cerebellar Ataxia W/o Cc/mcc
Chapter Diseases of the nervous system (G00-G99)
Block Systemic atrophies primarily affecting the central nervous system (G10-G14)
Parent G11 - Hereditary ataxia
ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD 9 Dx Code: 334.8 - Other spinocerebellar diseases (approximate)
ICD-10-CM Siblings (same level / similar specificity) of G11.3:
G11.0 - Congenital nonprogressive ataxia
G11.1 - Early-onset cerebellar ataxia
G11.2 - Late-onset cerebellar ataxia
G11.4 - Hereditary spastic paraplegia
G11.8 - Other hereditary ataxias
G11.9 - Hereditary ataxia, unspecified